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Items: 1 to 20 of 385

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129810insertion1nstd186human GRCh37 chr12: 125,520,734-125,520,734 , GRCh38.p12 chr12: 125,036,188-125,036,188 BRI3BP
    nsv5977940insertion1nstd209human GRCh38 chr12: 125,019,657-125,019,657 , GRCh37.p13 chr12: 125,504,203-125,504,203 BRI3BP
    nsv5976838insertion1nstd209human GRCh38 chr12: 125,036,158-125,036,158 , GRCh37.p13 chr12: 125,520,704-125,520,704 BRI3BP
    nsv5968365insertion1nstd209human GRCh38 chr12: 124,997,214-124,997,214 , GRCh37.p13 chr12: 125,481,760-125,481,760 BRI3BP
    nsv5946275copy number variation1nstd209human GRCh38 chr12: 125,040,194-125,046,496 , GRCh37.p13 chr12: 125,524,740-125,531,042 BRI3BP
    nsv5936264copy number variation1nstd209human GRCh38 chr12: 125,000,579-125,001,651 , GRCh37.p13 chr12: 125,485,125-125,486,197 BRI3BP
    nsv5932391copy number variation1nstd209human GRCh38 chr12: 124,999,447-124,999,640 , GRCh37.p13 chr12: 125,483,993-125,484,186 BRI3BP
    nsv5931681copy number variation1nstd209human GRCh38 chr12: 125,033,990-125,034,291 , GRCh37.p13 chr12: 125,518,536-125,518,837 BRI3BP
    nsv5851442copy number variation1nstd209human GRCh38 chr12: 125,000,368-125,002,667 , GRCh37.p13 chr12: 125,484,914-125,487,213 BRI3BP
    nsv5847666copy number variation1nstd209human GRCh38 chr12: 125,039,986-125,045,885 , GRCh37.p13 chr12: 125,524,532-125,530,431 BRI3BP
    nsv5703835mobile element insertion1nstd211human GRCh38 chr12: 125,014,053-125,014,053 , GRCh37.p13 chr12: 125,498,599-125,498,599 BRI3BP
    nsv5657978insertion1nstd207human GRCh38 chr12: 125,036,158-125,036,158 , GRCh37.p13 chr12: 125,520,704-125,520,704 BRI3BP
    nsv5657576insertion1nstd207human GRCh38 chr12: 124,999,872-124,999,872 , GRCh37.p13 chr12: 125,484,418-125,484,418 BRI3BP
    nsv5547509insertion1nstd206human GRCh38 chr12: 125,036,188-125,036,188 , GRCh37.p13 chr12: 125,520,734-125,520,734 BRI3BP
    nsv5512219copy number variation1nstd206human GRCh38 chr12: 125,039,961-125,046,497 , GRCh37.p13 chr12: 125,524,507-125,531,043 BRI3BP
    nsv5511898copy number variation1nstd206human GRCh38 chr12: 125,022,823-125,055,927 , GRCh37.p13 chr12: 125,507,369-125,540,473 LOC100131779, THRIL, 1 more genes
    nsv5510926copy number variation1nstd206human GRCh38 chr12: 125,008,375-125,009,352 , GRCh37.p13 chr12: 125,492,921-125,493,898 BRI3BP
    nsv5506320copy number variation1nstd206human GRCh38 chr12: 125,006,049-125,007,359 , GRCh37.p13 chr12: 125,490,595-125,491,905 BRI3BP
    nsv5502284copy number variation1nstd206human GRCh38 chr12: 124,999,807-125,002,697 , GRCh37.p13 chr12: 125,484,353-125,487,243 BRI3BP
    nsv5498360copy number variation1nstd206human GRCh38 chr12: 125,049,011-125,050,179 , GRCh37.p13 chr12: 125,533,557-125,534,725 BRI3BP
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